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Merck
CN

236241

Pentaerythritol

99%

Synonym(s):

2,2-Bis(hydroxymethyl)-1,3-propanediol

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About This Item

Linear Formula:
C(CH2OH)4
CAS Number:
Molecular Weight:
136.15
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
204-104-9
Beilstein/REAXYS Number:
1679274
MDL number:
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vapor pressure

<1 mmHg ( 20 °C)

Quality Level

assay

99%

bp

276 °C/30 mmHg (lit.)

mp

253-258 °C (lit.)

SMILES string

OCC(CO)(CO)CO

InChI

1S/C5H12O4/c6-1-5(2-7,3-8)4-9/h6-9H,1-4H2

InChI key

WXZMFSXDPGVJKK-UHFFFAOYSA-N

General description

Pentaerythritol is acrystalline , odour less white solid. The presence of neopentane core and four terminalhydroxyl groups makes it a versatile substrate for the synthesispolyfunctionalized compounds.

Application

Pentaerythritol can be used as a starting material to prepare four armed polyurethane prepolymers, which are applicable in the synthesis of UV cured polyurethane dispersions.

It can be used as an additive in the preparation of flame retardant polymers.

It can also be used as a precursor to synthesize polyethylene glycol/4,4′-diphenylmethane diisocyanate/pentaerythritol copolymer which is applicable as heat storage material.


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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

易制爆化学品

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Chin-Wen Chen et al.
Polymers, 12(9) (2020-09-10)
Bio-based unsaturated poly(butylene adipate-co-butylene itaconate) (PBABI) aliphatic copolyesters were synthesized with pentaerythritol (PE) as a modifier, observing the melting point, crystallization, and glass transition temperatures were decreased from 59.5 to 19.5 °C and 28.2 to -9.1 °C as an increase
Zhiming Zhang et al.
Organic & biomolecular chemistry, 9(24), 8220-8223 (2011-10-13)
A trimer of cholic acid made by linking three cholic acid molecules with pentaerythritol via click chemistry serves as the center of an artificial metallohydrolase after the complexation of the triazole groups with a Zn(2+) ion. The invertible amphiphilic cavity
Michael C Hacker et al.
Biomacromolecules, 9(6), 1558-1570 (2008-05-17)
In this study, we synthesized and characterized a series of macromers based on poly( N-isopropylacrylamide) that undergo thermally induced physical gelation and, following chemical modification, can be chemically cross-linked. Macromers with number average molecular weights typically ranging from 2000-3500 Da



Global Trade Item Number

SKUGTIN
236241-50G04061838785527